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Human Genetics
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December 1, 1994
Physical mapping in the region of the Bruton's tyrosine kinase and alpha-galactosidase A gene loci in proximal Xq22
A K Sweatman, L A Bradley, R C Lovering, et al.
Clinical Science (London, England : 1979)
|
December 1, 1983
Importance of platelet-free preparations for evaluating lymphocyte nucleotide levels in inherited or acquired immunodeficiency syndromes
A Goday, H A Simmonds, D R Webster, et al.
Immunology Letters
|
May 1, 1992
Identical point mutation leading to low levels of mannose binding protein and poor C3b mediated opsonisation in Chinese and Caucasian populations
R J Lipscombe, Y L Lau, R J Levinsky, et al.
Human Genetics
|
October 1, 1995
Screening for mutations causing X-linked severe combined immunodeficiency in the IL-2R gamma chain gene by single-strand conformation polymorphism analysis
P A Clark, T Lester, S Genet, et al.
Lancet (London, England)
|
June 29, 1991
Molecular basis of opsonic defect in immunodeficient children
M Sumiya, M Super, P Tabona, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1986
Correlations between purine levels, clinical and immunological status in ADA deficiency
H A Simmonds, L D Fairbanks, G S Morris, et al.
Clinical and Experimental Immunology
|
December 1, 1987
Heterogeneity of biochemical, clinical and immunological parameters in severe combined immunodeficiency due to adenosine deaminase deficiency
G Morgan, R J Levinsky, K Hugh-Jones, et al.
Journal of Medical Genetics
|
September 1, 1994
Trisomy X in a female member of a family with X linked severe combined immunodeficiency: implications for carrier diagnosis
T Lester, M de Alwis, P A Clark, et al.
Bioscience Reports
|
January 1, 1983
Rapid prenatal diagnosis of adenosine deaminase deficiency and other purine disorders using foetal blood
H A Simmonds, L D Fairbanks, D R Webster, et al.
Immunology
|
January 1, 1988
Intestinal hypersensitivity reactions in the rat. I. Uptake of intact protein, permeability to sugars and their correlation with mucosal mast-cell activation
M W Turner, P Boulton, J G Shields, et al.
Page
of 18
Search research articles
Search
Showing results (131-140 of 173) with videos related to
Sort By:
Page
of 18
Human Genetics
|
December 1, 1994
Physical mapping in the region of the Bruton's tyrosine kinase and alpha-galactosidase A gene loci in proximal Xq22
A K Sweatman, L A Bradley, R C Lovering, et al.
Clinical Science (London, England : 1979)
|
December 1, 1983
Importance of platelet-free preparations for evaluating lymphocyte nucleotide levels in inherited or acquired immunodeficiency syndromes
A Goday, H A Simmonds, D R Webster, et al.
Immunology Letters
|
May 1, 1992
Identical point mutation leading to low levels of mannose binding protein and poor C3b mediated opsonisation in Chinese and Caucasian populations
R J Lipscombe, Y L Lau, R J Levinsky, et al.
Human Genetics
|
October 1, 1995
Screening for mutations causing X-linked severe combined immunodeficiency in the IL-2R gamma chain gene by single-strand conformation polymorphism analysis
P A Clark, T Lester, S Genet, et al.
Lancet (London, England)
|
June 29, 1991
Molecular basis of opsonic defect in immunodeficient children
M Sumiya, M Super, P Tabona, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1986
Correlations between purine levels, clinical and immunological status in ADA deficiency
H A Simmonds, L D Fairbanks, G S Morris, et al.
Clinical and Experimental Immunology
|
December 1, 1987
Heterogeneity of biochemical, clinical and immunological parameters in severe combined immunodeficiency due to adenosine deaminase deficiency
G Morgan, R J Levinsky, K Hugh-Jones, et al.
Journal of Medical Genetics
|
September 1, 1994
Trisomy X in a female member of a family with X linked severe combined immunodeficiency: implications for carrier diagnosis
T Lester, M de Alwis, P A Clark, et al.
Bioscience Reports
|
January 1, 1983
Rapid prenatal diagnosis of adenosine deaminase deficiency and other purine disorders using foetal blood
H A Simmonds, L D Fairbanks, D R Webster, et al.
Immunology
|
January 1, 1988
Intestinal hypersensitivity reactions in the rat. I. Uptake of intact protein, permeability to sugars and their correlation with mucosal mast-cell activation
M W Turner, P Boulton, J G Shields, et al.
Page
of 18